Implant for transforaminal intracorporeal fusion

ABSTRACT

The invention relates to an implant for the transforaminal intracorporeal fusion of lumbar vertebral column segments. At least some sections of the surface areas that are in direct contact with the spinal column are provided with an anti-dislocation mechanism ( 1 ) while an attachment part ( 4 ) for a positioning instrument ( 10 ) is provided in or on the implant and holes ( 6 ) or hollow spaces are disposed in the implant for filling purposes. According to one embodiment of the invention, the attachment part is configured as a revolute joint. In a further embodiment, the implant member has the shape of a sickle, the curvature of which is oriented ventrally and the interior of which is oriented dorsally. The attachment part is located at one end of the sickle while the opposite end of the sickle has a beak-type, tapering shape ( 5 ). At least one filling hole is provided between the sickle walls.

This application is a continuation of co-pending U.S. patent applicationSer. No. 14/663,040 filed Mar. 19, 2015, which is a continuationapplication of U.S. patent application Ser. No. 13/959,370 filed Aug. 5,2013, which is a continuation application of U.S. patent applicationSer. No. 12/308,148 filed Jul. 6, 2009, now U.S. Pat. No. 8,506,629,which claims the benefit of International Application No.PCT/EP2005/000881 filed Jan. 28, 2005. The entire disclosure of thesedocuments is herein incorporated by reference into the presentapplication.

BACKGROUND

The invention related to an implant for the transforaminal interbodyfusion of lumbar vertebral column segments, wherein at least somesections of the surface areas coming into direct contact with thevertebral column are provided with a dislocation protection, whereinfurther an engagement part for a positioning instrument is provided inor on the implant, and holes or hollow spaces are disposed in theimplant for filling purposes.

Attempts are made to use minimal invasive surgery for spine operations.To this end, so-called PLIF (posterior lateral interbody fusion)operation techniques were developed. According to such an operationtechnique the intervertebral disc is removed through a posterior access,and the intervertebral space is filled with autologous bone. Thistechnique is based on Cloward, who was the first to carry through suchan operation in 1943. Further developments of the PLIF techniqueresulted in the application of a transforaminal access. This techniqueprovides for the dorsal, transforaminal introduction of titaniumcups—so-called cages—which are filled with autologous cancellous bone.At the same time, a dorsal instrumentation and stabilization is applied.The advantage of the briefly outlined method is that no transabdominalor retroperitoneal additional access has to be used.

The “Biotit Cage” of the company Ulrich serves to replace anintervertebral disc of the lumbar vertebral column. The cage is insertedthrough a dorsal access, with the application being possible in pairs orindividually. This prior cage is substantially U-shaped and comprises adislocation protection in the form of a striated structure. The implantmaterial of the aforementioned cage is titanium or a titanium alloy,respectively, so that relatively large radiological windows arenecessary to control the fusion.

Further known is a cage distributed by the company Stryker Orthopaedic,U.S.A., which is a cubic implant and can be implanted in pairs into theintervertebral space by an anterior as well as a posterior approach.

As regards the prior art, reference is additionally made to DE 43 28 062A1, which relates to an implant for the replacement of vertebral bodiesand/or the stabilization and fixation of the vertebral column. Thisimplant consists of an implant body which is pushed onto a support rodtransversely to the axis of the rod. The implant body according to DE 4328 062 A1 is provided with a surface structure bearing against thevertebral bodies adjacent to the implant, so as to achieve a mutualfixation of the adjacent surfaces of the implant body on the one handand the vertebral body on the other hand.

The prior art likewise includes height-adjustable vertebral bodyimplants for the replacement of one or more vertebral bodies, e.g.according to DE 44 23 257 A1, DE 195 19 101 A1 or DE 195 09 317 A1.However, the production of these height-adjustable implants is veryexpensive, and their handling is complicated.

In the German utility model DE 296 16 778 U1 a vertebral bodyreplacement is disclosed, which is inserted, for example, after avertebral body resection to replace the missing vertebral body. Suchreplacements are made of a body-compatible material, with the front endsforming an irregular edge and the wall of the replacement having holesto provide for enough space to receive bone substance.

To insert the replacement according to DE 296 16 77B U1, a tool having arelatively long shank is used, with the shank having a threaded journalon the free end thereof to be brought into engagement with a threadedhole of the sleeve-shaped body so as to insert the same into the spaceof the resected vertebral body, in the predefined position between twoadjacent vertebral bodies.

SUMMARY

Based on the foregoing it is the object of the invention to provide afurther developed implant for the transforaminal interbody fusion oflumbar vertebral column segments. The implant is to have a high primarystability and allows a simple operative procedure in use.

In one embodiment, there is an implant for the transforaminal interbodyfusion of lumbar vertebral column segments wherein at least somesections of the surface areas coming into direct contact with thevertebral column are provided with a dislocation protection, whereinfurther an engagement part for a positioning instrument is provided inor on the implant, and holes or hollow spaces are disposed in theimplant for filling purposes, and wherein the engagement part is formedas a pivot joint or hinge joint. In one embodiment, there is a specificpositioning instrument, wherein the insertion opening in the bolt has aninner thread.

Proceeding from an implant of which at least some sections of thesurface areas coming into direct contact with the vertebral column areprovided with a dislocation protection and which is provided with anengagement part for a positioning instrument, the further developedimplant body has the shape of a sickle, with the convexity of the sicklebeing oriented ventrally and the inner side of the sickle being orienteddorsally.

The specific engagement part, which acts like a pivot joint, is locatedon one end of the sickle, while the opposite end of the sickle has abeak-like, tapering shape which serves as an insertion aid. At least onefilling hole for receiving a large amount of bone substance is providedbetween the sickle walls of the implant body.

In one embodiment of the invention the engagement part is formed as arotatable or pivotable bolt received in a through bore, the bolt havingan insertion opening for an instrument which extends perpendicular tothe longitudinal axis.

The sickle end with the engagement part is provided with a recessserving as access to the bolt and to the insertion opening for theaforementioned positioning instrument.

Preferably, the implant is made of a bioelastic synthetic material,specifically polyetheretherketone (PEEK). However, other appropriateimplant materials are usable as well.

X-ray markers are incorporated in the bioelastic synthetic material. Inthe ventral, medial part these X-ray markers may be oriented vertically,while the orientation may be a horizontal, saggital one at the implanttip.

Moreover, it is possible according to the invention to construct thebolt as a rotary part made of an X-ray detectable material.

Preferably, the structures of the dislocation protection have the shapeof a truncated pyramid or truncated cone, or are realized in the form ofspherical, cut bodies.

In a preferred embodiment of the invention the insertion opening of thebolt has an inner thread.

The positioning instrument used for handling the above-described implantis comprised of a shank and a sleeve, wherein the sleeve receives a pinwith a threaded end and the threaded end is designed complementarilywith respect to the inner thread of the insertion opening in the bolt.

Moreover, the pin with the threaded end can be moved by a rotary motionto be longitudinally displaceable relative to the sleeve. At the leadingend of the sleeve a stopping face for the implant is provided, so thatthe implant held by the pin is fixable in the respective angularposition by means of the bolt and the stopping face through tensioning.

In a surprising manner it has shown that the use of the bioelasticsynthetic material PEEK provides for ideal conditions for a permanentfusion: The elastic properties similar to those of the bone prevent theimplant from sinking in and support the fusion tendency. At the sametime, the X-ray transparency ensures optimum postoperative diagnostics,namely without requiring, as compared to the prior art, largerradiological windows in the implant material.

Suitable, also relatively small and correspondingly positioned X-raymarkers made, for example, of titanium or a titanium alloy material,allow the localization of the implant at any time.

With respect to the application and use of the implant, reference ismade to the statements set forth below.

At first, the intervertebral disc space is emptied through atransforaminal access. To this end, appropriate grasping forceps orshaped curettes known per se are used.

After the diskectomy, the intervertebral disc space is distracted bymeans of special distracters to the desired height. A suitabledistraction height is reached as soon as the distractor is under tensionand a respectively stable feeling is achieved. After the distraction,the required implant size, specifically the height of the implant isverified by means of special test implants. The positioning instrumentaccording to the invention may already be used to hold these testimplants.

Prior to the implantation of the implant, the size of which has thenbeen ascertained, an appropriate material, e.g. cancellous bone, ispreferably filled into the intervertebral disc space ventrally and intothe opposite lateral side of the implant. The portion dorsally of theimplant is filled as well.

For the implant, which is to be filled as well, a filling aid is used,into which the implant is inserted. The filling aid adopts the outercontour of the implant and defines a support frame.

After a suitable angle between the instrument and the implant was foundby means of the positioning instrument and the stopping possibility, andafter this angle was subjected to a corresponding fixation, the implantis inserted into the intervertebral disc space. Due to the implantationcurve it is recommendable to adapt during the actual implantation theangle by a brief loosening motion, by making use of the advantageouseffects of the positioning instrument.

A final positioning may be achieved by means of suited straight or bentpush-pins. To obtain a correct implantation, the convex side of theimplant is oriented ventrally and the two implant ends are orienteddorsally. To obtain all desired advantageous effects, the implant shouldbe positioned as ventrally as possible. After the implantation, the restof the intervertebral disc space is filled, so as to ensure a reliablefusion.

The principle of the implant according to the invention is based on thetension of the annulus and the longitudinal ligaments in combinationwith a sufficient bone quality. In certain cases, an additionalstabilization should be obtained by means of a dorsal fixator.

As was mentioned before, the implant may be made of a syntheticmaterial, specifically of PEEK. This material is transparent to X-rays,and its mechanical properties are very similar to those of the body. Tofacilitate postoperative diagnostics, X-ray markers may be incorporatedinto the implant. A marker is located, for example, in the ventral,medial portion of the implant in vertical orientation, and anothermarker at the tip of the implant in horizontal, sagittal orientation.Additionally, the rotary part for receiving the instrument may act as anX-ray marker.

The invention shall be explained in more detail below by means of anembodiment and with the aid of figures.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows various representations of the sickle-shaped implantaccording to the invention, and

FIG. 2 shows a lateral view and a perspective representation of theimplant positioning instrument.

DETAILED DESCRIPTION

The surface areas of the implant for the transforaminal interbody fusionof lumbar vertebral column segments according to the embodiment, whichcome into direct contact with the vertebral column, have specificstructures 1 serving as a dislocation protection. These structures 1 canhave, for example, the shape of truncated pyramids or truncated cones,or may be realized in the form of cut, spherical bodies.

The implant body itself is sickle-shaped, whereby, in case of use, theconvexity of the sickle 2 is oriented ventrally and the inner side ofthe sickle 3 is oriented dorsally.

An engagement part 4 is provided on one end of the sickle, and the otherend of the sickle opposite to this engagement part has a tapering,beak-like shape 5.

At least one filling hole 6 is provided between the sickle walls.

The engagement part 4 is formed as a pivotable or rotatable bolt , whichis located in a corresponding recess 7 in the implant.

The bolt comprises an insertion opening 8 with an inner thread (notshown), which extends substantially perpendicular to the longitudinalaxis of the bolt.

The insertion opening 8 serves to receive a respective end 9 of thepositioning instrument 10 (FIG. 2).

In the implant body, which is preferably made of a synthetic material,various X-ray markers may be incorporated, which are not illustrated inthe figures, so that a postoperative localization of the implant can beachieved at any time.

According to FIG. 2 the positioning instrument 10 is comprised of ahandle 11 with a sleeve 12.

A pin with a threaded end (part 9) is guided in the sleeve 12, whereinthe threaded end is designed complementarily with respect to the innerthread of the insertion opening 8 in the bolt.

By a rotary motion on the cap 14 the pin 9 with the threaded end can bemoved.

At the leading end of the sleeve 12 a stopping face 13 for the implantis provided, so that the implant held by the pin 9 is fixable in therespective angular position by means of the bolt and the stopping face13.

1-11. (canceled)
 12. An implant for the transforaminal interbody fusionof lumbar vertebral column segments, comprising: a main body including afirst surface configured for disposal adjacent a first vertebral surfaceand a second surface configured for disposal adjacent a second vertebralsurface, the main body having a sickle shape and further including atleast one side wall, and a first end portion having a beak-like taperingand a second end portion situated opposite the first end portion, thesecond end portion having a throughbore formed therein, the throughboreconfigured to receive a bolt having a sidewall and an insertion openingformed in the sidewall extending through the bolt.
 13. An implantaccording to claim 12, wherein the throughbore is oriented transverselyin the main body in a direction between the first surface and the secondsurface and the main body having at least one filling hole adjacent toand separate from the throughbore.
 14. An implant according to claim 12,wherein the bolt is rotatably or pivotally received by atransversely-oriented throughbore.
 15. An implant according to claim 12,wherein the first and second surfaces include dislocation protectionelements having the shape of at least one of a truncated pyramid and atruncated cone.
 16. An implant according to claim 12, wherein theinsertion opening in the bolt has an inner thread.
 17. An implantaccording to claim 12, wherein the second end portion comprises anaccess recess in communication with the insertion opening formed in thebolt to allow a portion of a positioning instrument for positioning theimplant between vertebrae to pass therethrough and into the insertionopening of the bolt.
 18. An implant according to claim 12, wherein theimplant is made of a bioelastic synthetic material.
 19. An implantaccording to claim 18, wherein the bioelastic synthetic materialcomprises polyetheretherketone (PEEK).
 20. An implant according to claim12, wherein the implant is provided with X-ray markers.
 21. An implantaccording to claim 12, wherein the bolt is a rotary part made of anX-ray detectable material.
 22. An implant for the transforaminalinterbody fusion of lumbar vertebral column segments, comprising: a mainbody including a top surface configured for disposal adjacent a firstvertebral surface and a bottom surface situated opposite the top surfaceconfigured for disposal adjacent a second vertebral surface, the mainbody having a sickle shape and further including an inner side wall andan outer side wall situated opposite the inner side wall, and a firstend portion having a beak-like tapering and a second end portionsituated opposite the first end portion, the second end portion having athroughbore formed therein and oriented transversely in the main body ina direction between the top surface and the bottom surface and the mainbody having at least one filling hole adjacent to and separate from thethroughbore, the throughbore comprising a bolt having a side wall and aninsertion opening formed in the sidewall extending through the bolt. 23.An implant according to claim 22, wherein the bolt is rotatably orpivotally received by the transversely-oriented throughbore.
 24. Animplant according to claim 22, wherein the top and bottom surfacesinclude dislocation protection elements having the shape of at least oneof a truncated pyramid and a truncated cone.
 25. An implant according toclaim 22, wherein the insertion opening in the bolt has an inner thread.26. An implant according to claim 22, wherein the second end portioncomprises an access recess in communication with the insertion openingformed in the bolt to allow a portion of a positioning instrument forpositioning the implant between vertebrae to pass therethrough and intothe insertion opening of the bolt.
 27. An implant according to claim 22,wherein the implant is made of a bioelastic synthetic material.
 28. Animplant according to claim 27, wherein the bioelastic synthetic materialcomprises polyetheretherketone (PEEK).
 29. An implant according to claim22, wherein the implant is provided with X-ray markers.
 30. An implantaccording to claim 22, wherein the bolt is a rotary part made of anX-ray detectable material.
 31. An implant for the transforaminalinterbody fusion of lumbar vertebral column segments, comprising a mainbody and an engagement part, the main body including a first surfacehaving dislocation protection elements configured for engagement with afirst vertebra and a second surface situated opposite the top surfacehaving dislocation protection elements configured for engagement with asecond vertebra, the main body further including at least one side wall,and a first end portion and a second end portion situated opposite thefirst end portion and defining a first axis, the second end portionhaving a throughbore formed therein and oriented transversely to thefirst axis and the main body having at least one filling hole adjacentto and separate from the throughbore; the engagement part including abolt being rotatably disposed in the transversely-oriented throughbore,the bolt defining a longitudinal axis oriented transversely to the firstaxis and extending between the top surface and the bottom surface, thebolt having a side wall and an insertion opening formed thereinextending perpendicularly to the longitudinal axis.